Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/- | Ancestral: T | MAF: 0.02 (-)
Location

Chromosome 20:958163 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

20:g.958163delT

About this variant

This variant overlaps 2 transcripts and has 2506 individual genotypes.

Variation displays